Preis Heike, Eckart Rita A, Gudipati Rajani K, Heidrich Nadja, Brantl Sabine
Friedrich-Schiller-Universität Jena, Biologisch-Pharmazeutische Fakultät, AG Bakteriengenetik, Jena D-07743, Germany.
J Bacteriol. 2009 Sep;191(17):5446-57. doi: 10.1128/JB.00602-09. Epub 2009 Jun 19.
Regulatory small RNAs (sRNAs) in bacterial genomes have become a focus of research over the past 8 years. Whereas more than 100 such sRNAs have been found in Escherichia coli, relatively little is known about sRNAs in gram-positive bacteria. Using a computational approach, we identified two sRNAs in intergenic regions of the Bacillus subtilis genome, SR1 and SR2 (renamed BsrF). Recently, we demonstrated that SR1 inhibits the translation initiation of the transcriptional activator AhrC. Here, we describe detection of BsrF, its expression profile, and its regulation by CodY. Furthermore, we mapped the secondary structure of BsrF. BsrF is expressed in complex and minimal media in all growth phases in B. subtilis and, with a similar expression profile, also in Bacillus amyloliquefaciens. Neither overexpression nor deletion of bsrF affected the growth of B. subtilis. BsrF was found to be long-lived in complex and minimal media. Analysis of 13 putative transcription factor binding sites upstream of bsrF revealed only an effect for CodY. Here, we showed by using Northern blotting, lacZ reporter gene fusions, in vitro transcription, and DNase I footprinting that the transcription of bsrF is activated by CodY in the presence of branched-chain amino acids and GTP. Furthermore, BsrF transcription was increased 1.5- to 2-fold by glucose in the presence of branched-chain amino acids, and this increase was independent of the known glucose-dependent regulators. BsrF is the second target for which transcriptional activation by CodY has been discovered.
在过去8年里,细菌基因组中的调控小RNA(sRNA)已成为研究热点。尽管在大肠杆菌中已发现100多种此类sRNA,但对于革兰氏阳性菌中的sRNA却知之甚少。我们采用计算方法,在枯草芽孢杆菌基因组的基因间区域鉴定出两种sRNA,即SR1和SR2(后重新命名为BsrF)。最近,我们证明SR1可抑制转录激活因子AhrC的翻译起始。在此,我们描述了BsrF的检测、其表达谱及其受CodY的调控。此外,我们绘制了BsrF的二级结构。BsrF在枯草芽孢杆菌的所有生长阶段均在复杂培养基和基本培养基中表达,并且在解淀粉芽孢杆菌中也具有相似的表达谱。bsrF的过表达或缺失均未影响枯草芽孢杆菌的生长。发现BsrF在复杂培养基和基本培养基中寿命较长。对bsrF上游13个假定的转录因子结合位点进行分析,结果显示仅CodY有作用。在此,我们通过Northern印迹法、lacZ报告基因融合、体外转录和DNase I足迹法表明,在存在支链氨基酸和GTP的情况下,CodY可激活bsrF的转录。此外,在存在支链氨基酸的情况下,葡萄糖可使BsrF的转录增加1.5至2倍,且这种增加与已知的葡萄糖依赖性调节因子无关。BsrF是已发现的第二个受CodY转录激活的靶标。